(S)-2-Amino-5-methylhexanoic acid hydrochloride

98%

Reagent Code: #236585
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CAS Number 1330286-49-1

science Other reagents with same CAS 1330286-49-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 181.66 g/mol
Formula C₇H₁₆ClNO₂
badge Registry Numbers
MDL Number MFCD06795775
inventory_2 Storage & Handling
Storage Room temperature, inert gas

description Product Description

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of protease inhibitors and other bioactive molecules. Its branched-chain structure and stereochemistry make it valuable for designing drugs with high specificity and improved metabolic stability. Commonly employed in research for peptide mimetics and enzyme inhibitors where selective amino acid analogs are required. Also utilized in asymmetric synthesis to introduce defined stereocenters in complex organic molecules.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,750.00
inventory 1g
10-20 days ฿5,800.00
inventory 5g
10-20 days ฿22,250.00

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(S)-2-Amino-5-methylhexanoic acid hydrochloride
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Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of protease inhibitors and other bioactive molecules. Its branched-chain structure and stereochemistry make it valuable for designing drugs with high specificity and improved metabolic stability. Commonly employed in research for peptide mimetics and enzyme inhibitors where selective amino acid analogs are required. Also utilized in asymmetric synthesis to introduce defined stereocenters in complex organi

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of protease inhibitors and other bioactive molecules. Its branched-chain structure and stereochemistry make it valuable for designing drugs with high specificity and improved metabolic stability. Commonly employed in research for peptide mimetics and enzyme inhibitors where selective amino acid analogs are required. Also utilized in asymmetric synthesis to introduce defined stereocenters in complex organic molecules.

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